Gene: SCO2 ×
Source: UNIPROT ×
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs74315511
rs74315511
SCO2 ; NCAPH2
0.800 GeneticVariation UNIPROT Cooperation between COA6 and SCO2 in COX2 maturation during cytochrome c oxidase assembly links two mitochondrial cardiomyopathies. 25959673

2015
dbSNP: rs74315511
rs74315511
SCO2 ; NCAPH2
0.800 GeneticVariation UNIPROT Detection of mutations in LRPAP1, CTSH, LEPREL1, ZNF644, SLC39A5, and SCO2 in 298 families with early-onset high myopia by exome sequencing. 25525168

2014
dbSNP: rs74315511
rs74315511
SCO2 ; NCAPH2
0.800 GeneticVariation UNIPROT Mutations in SCO2 are associated with autosomal-dominant high-grade myopia. 23643385

2013
dbSNP: rs370130010
rs370130010
SCO2 ; NCAPH2
0.700 GeneticVariation UNIPROT Cooperation between COA6 and SCO2 in COX2 maturation during cytochrome c oxidase assembly links two mitochondrial cardiomyopathies. 25959673

2015
dbSNP: rs370130010
rs370130010
SCO2 ; NCAPH2
0.700 GeneticVariation UNIPROT Detection of mutations in LRPAP1, CTSH, LEPREL1, ZNF644, SLC39A5, and SCO2 in 298 families with early-onset high myopia by exome sequencing. 25525168

2014
dbSNP: rs370130010
rs370130010
SCO2 ; NCAPH2
0.700 GeneticVariation UNIPROT Mutations in SCO2 are associated with autosomal-dominant high-grade myopia. 23643385

2013
dbSNP: rs145100473
rs145100473
SCO2 ; NCAPH2
0.700 GeneticVariation UNIPROT

dbSNP: rs375954523
rs375954523
SCO2 ; NCAPH2
0.700 GeneticVariation UNIPROT

dbSNP: rs8139305
rs8139305
SCO2 ; NCAPH2
0.700 GeneticVariation UNIPROT